NDCFind

Buprenorphine And Naloxone 67877-0607-90

Package NDC

67877-0607-90

Product NDC: 67877-0607

Manufacturer
Ascend Laboratories, Llc
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
July 3, 2026
Listing Expires
December 31, 2027
Application
ANDA214930

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride2 mg/1
Naloxone Hydrochloride.5 mg/1

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]Partial Opioid Agonist [EPC]

Selected Package

67877-0607-90Selected

90 TABLET in 1 BOTTLE (67877-607-90)

Other packages for this product(2)

30 TABLET in 1 BOTTLE (67877-607-30)

3 BLISTER PACK in 1 CARTON (67877-607-84) / 10 TABLET in 1 BLISTER PACK